510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925660Substantially Equivalent

Kti Transparent Wound Dressing

Kingston Technologies, Inc., Dayton NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925660 is the FDA 510(k) clearance record for KTI TRANSPARENT WOUND DRESSING, cleared for Kingston Technologies, Inc. on under FDA product code MGP (Dressing, Wound And Burn, Occlusive). FDA records list 6 510(k) clearances for Kingston Technologies, Inc., from to . As of , FDA records show no recalls naming K925660.

Clearance record

Decision date
Received
(161 days to decision)
Product code
MGP Dressing, Wound And Burn, Occlusive
Device class
Unclassified
Review panel
Unknown
Applicant
Kingston Technologies, Inc. 2235 Rte. 130, Dayton NJ
510(k) summary
Statement
Third party review
No

Clearances, product code MGP

Trailing 12 months

FDA records hold no clearances under product code MGP in the trailing twelve months.

FDA records show no clearances under product code MGP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MGP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260